Warianty tytułu
Języki publikacji
Abstrakty
To evaluate potential interactive effects of metals and polycyclic aromatic hydrocarbons (PAHs) on biomarker responses, groups of the freshwater fish crucian carp (Carassius auratus) were exposed to single and binary combinations of copper (Cu) (0.01-0.16 mg L-1) with fluorene (Fl) or fluoranthene (Fluo) (2-10 mg kg⁻¹) for 96 h. Dose-dependent increases in the activities of phases I and II metabolic enzymes [7-ethoxyresorufin O-deethylase (EROD) and glutathione-S-transferase (GST), respectively] were observed in fish liver exposed to Fl and Fluo, but these enzyme activities did not differ significantly from the controls when co-treated with higher concentrations of Cu, suggesting an inhibiting interaction on the metabolic enzymes. Although Cu did not alter catalase (CAT) activity, CAT activity was decreased in fish liver exposed to the two PAHs alone or in combination with Cu. Although metallothionein (MT) content in gills was significantly increased following exposure to Cu alone or in combination with Fl and Fluo, the induction folds of MT decreased under co-exposure. Co-exposures to these chemicals invoked complex biomarker responses in fish liver and gills. These results highlight the need for careful consideration of the interactive effects of multiple environmental stressors on fish.
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Tom
Numer
Opis fizyczny
p.183-190,fig.,ref.
Twórcy
autor
- College of Hydraulic and Civil Engineering, XiZang Agricultural and Animal Husbandry College, Linzhi, 860000, China
- Key Laboratory of Integrated Regulation and Resources Development of Shallow Lakes of Ministry of Education, College of the Environment, Hohai University, Nanjing 210098, China
autor
- Key Laboratory of Integrated Regulation and Resources Development of Shallow Lakes of Ministry of Education, College of the Environment, Hohai University, Nanjing 210098, China
autor
- School of the Environment and Civil Engineering, Jiangnan University, Wuxi 214122, China
Bibliografia
- 1. KONG M., HANG X., WANG L., YIN H., ZHANG Y. Accumulation and risk assessment of heavy metals in sediments and zoobenthos (Bellamya aeruginosa and Corbicula fluminea) from Lake Taihu. Water Science and Technology, 73(1), 203, 2016.
- 2. SU H., WU F., GUO J., HU Y., FENG C., CHEN C., GIESY J.P. Distribution characteristics and risk assessments of PAHs in fish from Lake Taihu, China. Human and Ecological Risk Assessment, 21, 1753, 2015.
- 3. VARNOSFADERANY M.N., BAKHTIARI A.R., GU Z., CHU G. Distribution and characteristic of PAHs in sediments from the southwest Caspian Sea, Guilan Province, Iran. Water Science and Technology, 71, 1587, 2015.
- 4. LU G.H., WANG C., ZHU Z. The dose-response relationships for EROD and GST induced by polyaromatic hydrocarbons in Carassius auratus. Bulletin of Environmental Contamination and Toxicology, 82, 194, 2009.
- 5. REYNAUD S., DESCHAUX P. The effects of polycyclic aromatic hydrocarbons on the immune system of fish: a review. Aquatic Toxicology, 77, 229, 2006.
- 6. SFAKIANAKIS D.G., RENIERI E., KENTOURI M., TSATSAKIS A.M. Effect of heavy metals on fish larvae deformities: a review. Environmental Research, 137, 246, 2015.
- 7. GAUTHIER P.T., NORWOOD W.P., PREPAS E.E., PYLE G.G. Metal-PAH mixtures in the aquatic environment: A review of co-toxic mechanisms leading to more-thanadditive outcomes. Aquatic Toxicology, 154, 253, 2014.
- 8. STORELLI M.M., BARONE G., PERRONE V.G., STORELLI A. Risk characterization for polycyclic aromatic hydrocarbons and toxic metals associated with fish consumption. Journal of Food Composition and Analysis, 31, 115, 2013.
- 9. TZORAKI O., KARAOUZAS I., PATROLECCO L., SKOULIKIDIS N., NIKOLAIDIS N.P. Polycyclic aromatic hydrocarbons (PAHs) and heavy metal occurrence in bed sediments of a temporary river. Water, Air, & Soil Pollution, 226, 1, 2015.
- 10. WANG C., LU G., WANG P., WU H., QI P., LIANG Y. Assessment of environmental pollution of Taihu Lake by combining active biomonitoring and integrated biomarker response. Environmental Science & Technology, 45, 3746, 2011.
- 11. BENEDETTI M., MARTUCCIO G., FATTORINI D., CANAPA A., BARUCCA M., NIGRO M., REGOLI F. Oxidative and modulatory effects of trace metals on metabolism of polycyclic aromatic hydrocarbons in the Antarctic fish Trematomus bernacchii. Aquatic Toxicology, 85, 167, 2007.
- 12. TRAN D., FOURNIER E., DURRIEU G., MASSABUAU J.C. Copper detection in the Asiatic clam Corbicula fluminea: optimum valve closure response. Aquatic Toxicology, 65, 317, 2003.
- 13. YAN J., LIU J., SHI X., YOU X., CAO Z. Polycyclic aromatic hydrocarbons (PAHs) in water from three estuaries of China: Distribution, seasonal variations and ecological risk assessment. Marine Pollution Bulletin, 109, 471-479, 2016.
- 14. SÁEZ M. I., GARCÍA-MESA S., CASAS J.J., GUILGUERRERO J.L., VENEGAS-VENEGAS C.E., MORALES A.E., SUÁREZ M.D. Effect of sublethal concentrations of waterborne copper on lipid peroxidation and enzymatic antioxidant response in Gambusia holbrooki. Environmental Toxicology and Pharmacology, 36, 125, 2013.
- 15. WILLETT K.L., WASSENBERG D., LIENESCH L., REICHERT W., DI GIULIO R.T. In vivo and in vitro inhibition of CYP1A-dependent activity in Fundulus heteroclitus by the polynuclear aromatic hydrocarbon fluoranthene. Toxicology and Applied Pharmacology, 177, 264, 2001.
- 16. FRASCO M.F., GUILHERMINO L. Effects of dimethoate and beta-naphthoflavone on selected biomarkers of Poecilia reticulata. Fish Physiology and Biochemistry, 26, 149, 2002.
- 17. GOTH L. A simple method for determination of serum catalase activity and revision of reference range. Clinica Chimica Acta, 196, 143, 1991.
- 18. ONOSAKA S., CHERIAN M.G. Comparison of metallothionein determination by polarographic and cadmium-saturation methods. Toxicology and Applied Pharmacology, 63, 270, 1982.
- 19. BRADFORD M.M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry, 72, 248, 1976.
- 20. WESSEL N., MÉNARD D., PICHAVANT-RAFINI K., OLLIVIER H., LE GOFF J., BURGEOT T., AKCHA F. Genotoxic and enzymatic effects of fluoranthene in microsomes and freshly isolated hepatocytes from sole (Solea solea). Aquatic Toxicology, 108, 33, 2012.
- 21. MATSON C.W., TIMME-LARAGY A.R., DI GIULIO R.T. Fluoranthene, but not benzo[a]pyrene, interacts with hypoxia resulting in pericardial effusion and lordosis in developing zebrafish. Chemosphere, 74, 149, 2008.
- 22. KOPECKA-PILARCZYK J., CORREIA A.D. Biochemical response in gilthead seabream (Sparus aurata) to in vivo exposure to pyrene and fluorene. Journal of Experimental Marine Biology and Ecology, 372, 49, 2009.
- 23. OWEN S.F., GILTROW E., HUGGETT D.B., HUTCHINSON T.H., SAYE J., WINTER M.J., SUMPTER J.P. Comparative physiology, pharmacology and toxicology of β-blockers: mammals versus fish. Aquatic Toxicology, 82, 145, 2007.
- 24. SHAILAJA M.S., D’SILVA C. Evaluation of impact of PAH on a tropical fish, Oreochromis mossambicus using multiple biomarkers. Chemosphere, 53, 835, 2003.
- 25. MELA M., GUILOSKI I.C., DORIA H.B., RABITTO I.S., DA SILVA C.A., MARASCHI A.C., PRODOCIMO V., FREIRE C.A., RANDI M.A.F., OLIVEIRA RIBEIRO C.A. SILVA DE ASSIS H.C. Risks of waterborne copper exposure to a cultivated freshwater Neotropical catfish (Rhamdia quelen). Ecotoxicology and Environmental Safety, 88, 108, 2013.
- 26. SANCHEZ W., PALLUEL O., MEUNIER L., COQUERY M., PORCHER J.M., AIT-AISSA S. Copper-induced oxidative stress in three-spined stickleback: relationship with hepatic metal levels. Environmental Toxicology and Pharmacology, 19, 177, 2005.
- 27. VIEIRA L.R., GRAVATO C., SOARES A.M.V.M., MORGADO F., GUILHERMINO L. Acute effects of copper and mercury on the estuarine fish Pomatoschistus microps: linking biomarkers to behaviour. Chemosphere, 76, 1416, 2009.
- 28. DING J., LU G., LIANG Y. Evaluation of the interactive effects of lead, zinc and benzo(k)fluoranthene on crucian carp, Carassius carassius, using a multiple biomarker approach. Bulletin of Environmental Contamination and Toxicology, 92, 534, 2014.
- 29. BOZCAARMUTLU A., ARINÇ E. Inhibitory effects of divalent metal ions on liver microsomal 7-ethoxyresorufin O-deethylase (EROD) activity of leaping mullet. Marine Environmental Research, 58, 521, 2004.
- 30. GHOSH M.C., GHOSH R., RAY A.K. Impact of copper on biomonitoring enzyme ethoxyresorufi n-o-deethylase in cultured catfish hepatocytes. Environmental Research, 86, 167, 2001.
- 31. TRAVEN L., MIĆOVIĆ V., LUŠIĆ D.V., SMITAL T. The responses of the hepatosomatic index (HSI), 7-ethoxyresorufin-O-deethylase (EROD) activity and glutathione-S-transferase (GST) activity in sea bass (Dicentrarchus labrax, Linnaeus 1758) caged at a polluted site: implications for their use in environmental risk assessment. Environmental Monitoring and Assessment, 185, 9009, 2013.
- 32. MOURENTE G., DIAZ-SALVAGO E., BELL J.G., TOCHER D.R. Increased activities of hepatic antioxidant defence enzymes in juvenile gilthead sea bream (Sparus aurata L.) fed dietary oxidised oil: attenuation by dietary vitamin E. Aquaculture, 214, 343, 2002.
- 33. LU G.H., CHEN W., LI Y., ZHU Z. Effects of PAHs on biotransformation enzymatic activities in fish. Chemical Research in Chinese Universities, 27, 413, 2011.
- 34. RODRIGUES A.P., LEHTONEN K.K., GUILHERMINO L., GUIMARÃES L. Exposure of Carcinus maenas to waterborne fluoranthene: accumulation and multibiomarker responses. Science of the Total Environment, 443, 454, 2013.
- 35. ATLI G., CANLI M. Response of antioxidant system of freshwater fish Oreochromis niloticus to acute and chronic metal (Cd, Cu, Cr, Zn, Fe) exposures. Ecotoxicology and Environmental Safety, 73, 1884, 2010.
- 36. ATLI G., GROSELL M. Characterization and response of antioxidant systems in the tissues of the freshwater pond snail (Lymnaea stagnalis) during acute copper exposure. Aquatic Toxicology, 176, 38, 2016.
- 37. SALMON A.B., RICHARDSON A., PÉREZ V.I. Update on the oxidative stress theory of aging: does oxidative stress play a role in aging or healthy aging? Free Radical Biology and Medicine, 48, 642-655, 2010.
- 38. BUET A., BANAS D., VOLLAIRE Y., COULET E., ROCHE H. Biomarker responses in European eel (Anguilla anguilla) exposed to persistent organic pollutants. A field study in the Vaccarès lagoon (Camargue, France). Chemosphere, 65, 1846, 2006.
- 39. KOPECKA-PILARCZYK J., CORREIA A.D. Biochemical response in gilthead seabream (Sparus aurata) to in vivo exposure to a mix of selected PAHs. Ecotoxicology and Environmental Safety, 72, 1296, 2009.
- 40. ATLI G., CANLI M. Enzymatic responses to metal exposures in a freshwater fish Oreochromis niloticus. Comparative Biochemistry and Physiology, 145C, 282, 2007.
- 41. SIMONATO J.D., MELA M., DORIA H.B., GUILOSKI I.C., RANDI M.A., CARVALHO P.S., MELETTI P.C., SILVA DE ASSIS H.C., BIANCHINI A., MARTINEZ C.B.R. Biomarkers of waterborne copper exposure in the Neotropical fish Prochilodus lineatus. Aquatic Toxicology, 170, 31, 2016.
- 42. PIAZZA R.S., TREVISAN R., FLORES-NUNES F., TOLEDO-SILVA G., WENDT N., MATTOS J.J., LIMA D., TANIGUCHI S., SASAKI S.T., MELLO Á.C.P., ZACCHI F.L., SERRANO M.A.S., GOMES C.H.A.M., BÍCEGO M.C., DE ALMEIDA E.A., BAINY A.C.D. Exposure to phenanthrene and depuration: Changes on gene transcription, enzymatic activity and lipid peroxidation in gill of scallops Nodipecten nodosus. Aquatic Toxicology, 177, 146-155, 2016.
- 43. DANG Z., LOCK R.A., FLIK G., BONGA, S.E.W. Metallothionein response in gills of Oreochromis mossambicus exposed to copper in fresh water. American Journal of Physiology-Regulatory, 277, R320, 1999.
- 44. NAJI A., ISMAIL A., KAMRANI E., SOHRABI T. Correlation of MT levels in livers and gills with heavy metals in wild tilapia (Oreochromis mossambicus) from the Klang River, Malaysia. Bulletin of Environmental Contamination and Toxicology, 92, 674, 2014.
- 45. DE SMET H., DE WACHTER B., LOBINSKI R., BLUST R. Dynamics of (Cd, Zn)-metallothioneins in gills, liver and kidney of common carp Cyprinus carpio during cadmium exposure. Aquatic Toxicology, 52, 269, 2001.
- 46. SEVCIKOVA M., MODRA H., BLAHOVA J., DOBSIKOVA R., PLHALOVA L., ZITKA O., HYNEK D., KIZEK R., SKORIC M., SVOBODOVA Z. Biochemical, haematological and oxidative stress responses of common carp (Cyprinus carpio L.) after sub-chronic exposure to copper. Veterinarni Medicina, 61, 35, 2016.
- 47. ROSE S., VINCENT S., MEENA B., SURESH A., MANI R. Metallothionein induction in fresh water catfish Clarias gariepinus on exposure to cadmium. International Journal of Pharmacy and Pharmaceutical Sciences, 6, 377, 2014.
- 48. VAN DEN HURK P., FAISAL M., ROBERTS JR M.H. Interactive effects of cadmium and benzo[a]pyrene on metallothionein induction in mummichog (Fundulus heteroclitus). Marine Environmental Research, 50, 83, 2000.
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
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